Overview
David Weaver is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Weaver is highly rated in 13 conditions, according to our data. His top areas of expertise are Weaver Syndrome, Chromosome 6q Deletion, Chromosome 6p Duplication, and Achard Syndrome. Dr. Weaver is currently accepting new patients.
His clinical research consists of co-authoring 38 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- CareSource
- Humana
Locations
975 W Walnut St, Indianapolis, IN 46202
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
1 Clinical Trials
University Family Physicians, Inc.
Brett Graham is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Graham is highly rated in 8 conditions, according to our data. His top areas of expertise are MELAS Syndrome, Mitochondrial Complex 1 Deficiency, Hypotonia, and Smith-Magenis Syndrome. Dr. Graham is currently accepting new patients.
University Family Physicians, Inc.
Clair Francomano is a Medical Genetics provider in Indianapolis, Indiana. Dr. Francomano is highly rated in 5 conditions, according to our data. Her top areas of expertise are Ehlers-Danlos Syndrome (EDS), Vascular Ehlers-Danlos Syndrome (VEDS), Brittle Cornea Syndrome, Musculocontractural Ehlers-Danlos Syndrome (mcEDS), and Spinal Fusion. Dr. Francomano is currently accepting new patients.
University Family Physicians, Inc.
Bryan Hainline is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Hainline is highly rated in 38 conditions, according to our data. His top areas of expertise are Phenylketonuria (PKU), Adrenoleukodystrophy (ALD), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Hainline is currently accepting new patients.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Weaver Syndrome
- Advanced
- Achard Syndrome
- Acromicric Dysplasia
- Aplasia Cutis Congenita
- Arachnodactyly
- Chromosome 6p Duplication
- Chromosome 6q Deletion
- Experienced
- Achalasia Microcephaly Syndrome
- Achondroplasia
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly Taurinuria